Amir Gizatullin 1 , Jonathan Becker 2 , Daut Islamov 3 , Nikita Serov 1 , Siegfried Schindler 2 , Alexander Klimovitskii 1 , Valery Shtyrlin 1 . Show Affiliations »
Abstract
The title hydrated copper(I)-l-cysteine-chloride complex has a polymeric structure of composition {[Cu16(CysH2)6Cl16]·xH2O} n [CysH2 = HO2CCH(NH3 +)CH2S- or C3H7NO2S], namely, poly[[tetra-μ3-chlorido-deca-μ2-chlorido-di-chlorido-hexa-kis-(μ4-l-cysteinato)hexa-deca-copper] polyhydrate]. The copper atoms are linked by thiol-ate groups to form Cu12S6 nanoclusters that take the form of a tetra-kis cubocta-hedron, made up of a Cu12 cubo-octa-hedral subunit that is augmented by six sulfur atoms that are located symmetrically atop of each of the Cu4 square units of the Cu12 cubo-octa-hedron. The six S atoms thus form an octa-hedral subunit themselves. The exterior of the Cu12S6 sphere is decorated by chloride ions and trichlorocuprate units. Three chloride ions are coordinated in an irregular fashion to trigonal Cu3 subunits of the nanocluster, and four trigonal CuCl3 units are bonded via each of their chloride ions to a copper ion on the Cu12S6 sphere. The trigonal CuCl3 units are linked via Cu2Cl2 bridges covalently connected to equivalent units in neighboring nanoclusters. Four such connections are arranged in a tetra-hedral fashion, thus creating an infinite diamond-like net of Cu12S6Cl4(CuCl3)4 nanoclusters. The network thus formed results in large channels occupied by solvent mol-ecules that are mostly too ill-defined to model. The content of the voids, believed to be water mol-ecules, was accounted for via reverse Fourier-transform methods using the SQUEEZE algorithm [Spek (2015 ▸). Acta Cryst. C71, 9-18]. The protonated amino groups of the cysteine ligands are directed away from the sphere, forming N-H⋯Cl hydrogen bonds with chloride-ion acceptors of their cluster. The protonated carb-oxy groups point outwards and presumably form O-H⋯O hydrogen bonds with the unresolved water mol-ecules of the solvent channels. Disorder is observed in one of the two crystallographically unique [Cu16(CysH2)6Cl16] segments for three of the six cysteine anions. © Gizatullin et al. 2021.
The title hydrated copper(I)-l-cysteine-chloride complex has a polymeric structure of composition {[n class="Chemical">Cu 16(
CysH2 )6Cl16]·x
H2O }
n [CysH2 =
HO2 CCH(NH3 +)
CH2S - or C3H7
NO2S ], namely, poly[[tetra-μ3-chlorido-deca-μ2-chlorido-di-chlorido-hexa-kis-(μ4-l-cysteinato)hexa-deca-
copper ] polyhydrate]. The
copper atoms are linked by
thiol -ate groups to form
Cu12S6 nanoclusters that take the form of a tetra-kis
cu bocta-hedron, made up of a
Cu 12
cu bo-octa-hedral subunit that is augmented by six
sulfur atoms that are located symmetrically atop of each of the
Cu 4 square units of the
Cu 12
cu bo-octa-hedron. The six S atoms thus form an octa-hedral subunit themselves. The exterior of the
Cu12S6 sphere is decorated by
chloride ions and
trichlorocuprate units. Three
chloride ions are coordinated in an irregular fashion to trigonal
Cu 3 subunits of the nanocluster, and four trigonal
CuCl3 units are bonded via each of their
chloride ions to a
copper ion on the
Cu12S6 sphere. The trigonal
CuCl3 units are linked via
Cu2Cl2 bridges covalently connected to equivalent units in neighboring nanoclusters. Four such connections are arranged in a tetra-hedral fashion, thus creating an infinite diamond-like net of
Cu12S6Cl4 (
CuCl3 )4 nanoclusters. The network thus formed results in large channels oc
cu pied by solvent mol-e
cu les that are mostly too ill-defined to model. The content of the voids, believed to be
water mol-e
cu les, was accounted for via reverse Fourier-transform methods using the SQUEEZE algorithm [Spek (2015 ▸). Acta Cryst. C71, 9-18]. The protonated amino groups of the
cysteine ligands are directed away from the sphere, forming N-H⋯
Cl hydrogen bonds with
chloride -ion acceptors of their cluster. The protonated
carb -
oxy groups point outwards and presumably form O-H⋯O
hydrogen bonds with the unresolved
water mol-e
cu les of the solvent channels. Disorder is observed in one of the two crystallographically unique [
Cu 16(
CysH2 )6Cl16] segments for three of the six
cysteine anions. © Gizatullin et al. 2021.
Entities: CellLine
Chemical
Disease
Species
Keywords:
SQUEEZE procedure; cage structure; copper(I); crystal structure; cysteine; metal–organic framework
Year: 2021
PMID: 33936751 PMCID: PMC8025850 DOI: 10.1107/S2056989021002012
Source DB: PubMed Journal: Acta Crystallogr E Crystallogr Commun